trialkyl
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trialkyl — tri·alkyl … English syllables
trialkyl — (ˈ)trī+ adjective Etymology: tri + alkyl : containing three alkyl groups especially in place of hydrogen … Useful english dictionary
Phosphoryl chloride — Phosphoryl chloride … Wikipedia
Hydroboration-oxidation reaction — In organic chemistry, the hydroboration oxidation reaction is a two step organic chemical reaction that converts an alkene into a neutral alcohol by the net addition of water across the double bond. [cite book author = Loudon, Marc G. year = 2002 … Wikipedia
PUREX — is the de facto standard aqueous nuclear reprocessing method for the recovery of uranium and plutonium from used nuclear fuel. It is based on liquid liquid extraction ion exchange. For other methods of reprocessing, see nuclear… … Wikipedia
Michaelis-Arbuzov reaction — The Michaelis Arbuzov reaction is the chemical reaction of a trialkyl phosphite and an alkyl halide to form a phosphonate.The reaction was discovered by August Michaelis in 1898 [cite journal | author = Michaelis, A.; Kaehne, R. | journal =… … Wikipedia
Organoborane — PropertiesThe C B bond has low polarity (the difference in electronegativity 2.55 for carbon and 2.04 for boron) and therefore alkyl boron compounds are in general stable though easily oxidized. Vinyl groups and aryl groups donate electrons and… … Wikipedia
Baylis-Hillman reaction — The Baylis Hillman reaction is an organic reaction of an aldehyde and an α,β unsaturated electron withdrawing group catalyzed by DABCO (1,4 diazabicyclo [2.2.2] octane) to give an allylic alcohol [Baylis, A. B.; Hillman, M. E. D. German Patent… … Wikipedia
Homoleptic — In inorganic chemistry, a homoleptic chemical compound is a metal compound with all ligands identical. [GoldBookRef | title = homoleptic | file = H02850] The term uses a homo prefix to indicate that something is the same for all. Examples *… … Wikipedia
Barton-McCombie deoxygenation — The Barton McCombie deoxygenation is an organic reaction in which an hydroxy functional group in an organic compound is replaced by a hydride to give an alkyl group [cite journal author = Barton, D. H. R.; McCombie, S. W. journal = J. Chem. Soc … Wikipedia
